Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g07040 | A10 | 3859282 | C | T | missense_variant | MODERATE | c.713G>A|p.Gly238Glu |
S40 S49 |
2 | BAA10g07040 | A10 | 3860253 | G | A | splice_region_variant&synonymous_variant | LOW | c.51C>T|p.Phe17Phe |
S9 |
3 | BAA10g07040 | A10 | 3863439 | C | T | upstream_gene_variant | MODIFIER | c.-3136G>A| |
S35 |
4 | BAA10g07040 | A10 | 3864188 | C | T | upstream_gene_variant | MODIFIER | c.-3885G>A| |
S260 |
5 | BAA10g07040 | A10 | 3864307 | C | T | upstream_gene_variant | MODIFIER | c.-4004G>A| |
S121 |
6 | BAA10g07040 | A10 | 3864373 | G | A | upstream_gene_variant | MODIFIER | c.-4070C>T| |
S105 S106 |
7 | BAA10g07040 | A10 | 3865124 | C | T | upstream_gene_variant | MODIFIER | c.-4821G>A| |
S132 S137 S215 S89 |